# Pemetrexed

NDC: 63323-134
Generic name: PEMETREXED DISODIUM
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220525

FDA application: ANDA090384

## Active ingredients

- PEMETREXED DISODIUM: 100 mg/4mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-134"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-134
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae77f00f-d43b-4b75-afd5-a2a9cb7138da